van Spijk Julia N, Beckmann Katrin, Wehrli Eser Meret, Stirn Martina, Steuer Andrea E, Saleh Lanja, Schoster Angelika
Equine Department, Vetsuisse Faculty, University of Zurich, Winterthurerstrasse 260, CH-8057 Zurich, Switzerland.
Department of Small Animals, Vetsuisse Faculty, University of Zurich, Winterthurerstrasse 260, CH-8057 Zurich, Switzerland.
Antibiotics (Basel). 2023 May 5;12(5):854. doi: 10.3390/antibiotics12050854.
Neuro- and nephrotoxicity of polymyxins are known but clinical studies in horses are lacking. The aim of this study was to describe neurogenic and nephrogenic side effects of hospitalized horses receiving Polymyxin B (PolyB) as part of their treatment plan. Twenty horses diagnosed with surgical colic ( = 11), peritonitis ( = 5), typhlocolitis ( = 2), pneumonia, and pyometra (each = 1) were included. Antimicrobial treatment was randomized to GENTA (gentamicin 10 mg/kg bwt q24 h IV, penicillin 30.000 IU/kg q6 h IV) or NO GENTA (marbofloxacin 2 mg/kg bwt q24 h IV, penicillin 30.000 IU/kg q6 h IV). The duration of PolyB treatment ranged from 1 to 4 days. Clinical and neurological examinations were performed, and serum PolyB concentrations were measured daily during and three days following PolyB treatment. Urinary analysis, plasma creatinine, urea and SDMA were assessed every other day. Video recordings of neurological examinations were graded by three blinded observers. All horses showed ataxia during PolyB treatment in both groups (median maximum ataxia score of 3/5, range 1-3/5). Weakness was detected in 15/20 (75%) horses. In 8/14 horses, the urinary γ-glutamyltransferase (GGT)/creatinine ratio was elevated. Plasma creatinine was mildly elevated in 1/16 horses, and SDMA in 2/10 horses. Mixed-model analysis showed a significant effect of time since last PolyB dose ( = 0.0001, proportional odds: 0.94) on the ataxia score. Ataxia and weakness should be considered as reversible adverse effects in hospitalized horses receiving PolyB. Signs of tubular damage occurred in a considerable number of horses; therefore, the nephrotoxic effect of polymyxins should be considered and urinary function monitored.
多粘菌素的神经毒性和肾毒性是已知的,但缺乏针对马匹的临床研究。本研究的目的是描述接受多粘菌素B(PolyB)作为治疗方案一部分的住院马匹的神经源性和肾源性副作用。纳入了20匹被诊断为手术性绞痛(n = 11)、腹膜炎(n = 5)、盲结肠炎(n = 2)、肺炎和子宫积脓(各n = 1)的马匹。抗菌治疗随机分为庆大霉素组(庆大霉素10 mg/kg体重,静脉注射,每24小时一次;青霉素30000 IU/kg,静脉注射,每6小时一次)或非庆大霉素组(马波沙星2 mg/kg体重,静脉注射,每24小时一次;青霉素30000 IU/kg,静脉注射,每6小时一次)。PolyB治疗持续时间为1至4天。进行了临床和神经学检查,并在PolyB治疗期间及治疗后三天每天测量血清PolyB浓度。每隔一天评估尿液分析、血浆肌酐、尿素和对称二甲基精氨酸(SDMA)。神经学检查的视频记录由三名不知情的观察者进行评分。两组中所有马匹在PolyB治疗期间均出现共济失调(最大共济失调评分中位数为3/5,范围为1 - 3/5)。在15/20(75%)的马匹中检测到虚弱。在8/14的马匹中,尿γ-谷氨酰转移酶(GGT)/肌酐比值升高。1/16的马匹血浆肌酐轻度升高,2/10的马匹SDMA升高。混合模型分析显示,自上次PolyB给药后的时间(P = 0.0001,比例比:0.94)对共济失调评分有显著影响。共济失调和虚弱应被视为接受PolyB治疗的住院马匹的可逆性不良反应。相当数量的马匹出现肾小管损伤迹象;因此,应考虑多粘菌素的肾毒性并监测尿液功能。